美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
70518-2104-9	70518-2104	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20250701	N/A	ANDA	ANDA078235	REMEDYREPACK INC.	TOPIRAMATE	100 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2104-9)
80425-0092-1	80425-0092	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Advanced Rx Pharmacy of Tennessee, LLC	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0092-1)
80425-0092-2	80425-0092	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Advanced Rx Pharmacy of Tennessee, LLC	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0092-2)
80425-0092-3	80425-0092	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240814	N/A	ANDA	ANDA078235	Advanced Rx Pharmacy of Tennessee, LLC	TOPIRAMATE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0092-3)
82009-137-05	82009-137	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230724	N/A	ANDA	ANDA078235	Quallent Pharmaceuticals Health LLC	TOPIRAMATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-137-05)